Canonical Allele Identifier: PA2741808980
Gene: COMP HGNC NCBI

Linked Data

ClinVar Variation Id: 2755647
ClinVar RCV Id: RCV003571406
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000086.2:p.Thr575Ser
CA404879358
NM_000095.3:c.1724C>G
CA404879360
NM_000095.3:c.1723A>T